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Sr. Embedded Software EngineerDormont Manufacturing Company • Alameda, California, United States
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Sr. Embedded Software Engineer

Dormont Manufacturing Company
  • US
    Alameda, California, United States
  • US
    Alameda, California, United States
Jetzt Bewerben

Über

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.
JOB DESCRIPTION: The Opportunity:
The Sr Embedded Software Engineer oversees the design, development, and validation of software for embedded systems, ensuring compliance with FDA requirements. They play a crucial role in software design, coding, and validation, address moderate scope problems, and participate in software development activities under guidance and mentoring junior engineers. Adherence to FDA-compliant Design Control procedures and proficiency in software implementation are key aspects of the role.
What you’ll work on
Design and implement software in current programming languages (e.g. C, C++, C#, python).
Working from requirement specifications, develops, maintains, and updates detailed design and interface specifications.
Participates in and supports the implementation, development, enhancements, and modifications to software source code, scripts, and procedures.
Debugs, troubleshoots, and isolates software problems as well as offer strategic solutions, analysis, and advice regarding identified issues for future development.
Assist in the evaluation of selected designs through testing and full documentation of the results.
Work on problems of moderate scope where analysis of situations or data requires evaluation of identifiable factors.
Exercise judgment within defined procedures and practices to determine appropriate action.
Participate in software development, verification and validation following the guidance of software lead.
Follow approved Design Control procedures for software development in accordance with FDA guidelines.
Contributes to and supports writing, updating, developing and maintaining Hazard/Risk analysis specifications.
Contributes to and supports root-cause analysis of failures.
Required Qualifications
Minimum 7 years of related experience or Master’s Degree with 4+ years of related experience
Excellent written and verbal communication skills
Strong familiarity with current development tools (IDEs, debuggers, unit test frameworks)
Preferred Qualifications
Experience with middleware frameworks, protocol stacks, or system-level software. Examples: USB stack, BLE stack, TCP/IP, file systems, etc.
Experience building end-to-end systems (firmware → middleware → application)
Experience testing software is a plus
Knowledge of design controls and regulations for medical device development is a plus
Knowledge of the principles of quality software engineering as described by software lifecycle development processes that are consistent with ISO, IEEE, or other FDA recognized standards is a plus
Experience with software development life cycle processes is a plus
The base pay for this position is $100,000.00 – $200,000.00
In specific locations, the pay range may vary from the range posted.
JOB FAMILY: Product Development
DIVISION: ADC Diabetes Care
LOCATION: United States > Alameda : 1360-1380 South Loop Road
ADDITIONAL LOCATIONS: United States > Milpitas : 1820 McCarthy Blvd
WORK SHIFT: Standard
TRAVEL: Not specified
MEDICAL SURVEILLANCE: Not Applicable
SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
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  • Alameda, California, United States

Sprachkenntnisse

  • English
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